Canonical Allele Identifier: CA490946363

Gene: ITGA11

Linked Data

• MyVariant Identifiers: chr15:g.68628176T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.68335838T>G , CM000677.2:g.68335838T>G	GRCh38
NC_000015.9:g.68628176T>G , CM000677.1:g.68628176T>G	GRCh37
NC_000015.8:g.66415230T>G	NCBI36
NG_046911.1:g.101323A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000315757.9:c.1284A>C MANE Select	ENSP00000327290.7:p.Thr428=
ENST00000315757.8:c.1284A>C	ENSP00000327290.7:p.Thr428=
ENST00000423218.6:c.1284A>C	ENSP00000403392.2:p.Thr428=
ENST00000566429.1:n.197-24A>C
ENST00000569346.5:n.263A>C
NM_001004439.1:c.1284A>C	NP_001004439.1:p.Thr428=
XM_005254228.2:c.978A>C	XP_005254285.1:p.Thr326=
XM_011521363.1:c.1077A>C	XP_011519665.1:p.Thr359=
XM_005254228.3:c.978A>C	XP_005254285.1:p.Thr326=
XM_011521363.2:c.1077A>C	XP_011519665.1:p.Thr359=
NM_001004439.2:c.1284A>C MANE Select	NP_001004439.1:p.Thr428=